Applicability of Home-based Exercise Programs in Physiotherapy
Investigation of Feasibility and Effectiveness of Home-Based Exercise Programs in Physiotherapy According to Disease Status: A Randomized Controlled Multicenter Study Protocol
1 other identifier
observational
237
1 country
1
Brief Summary
Aim: In this study, the types of home-based exercise programs prepared for patients receiving physiotherapy services in different rehabilitation institutions; It is aimed to examine the applicability and effectiveness advantages according to disease status, age, gender, socioeconomic level, education level, confidence in the home program, and functional independence level. Study type: observational study Research question; To what extent do patients participate in home-based exercise programs?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 16, 2023
CompletedStudy Start
First participant enrolled
November 17, 2023
CompletedFirst Posted
Study publicly available on registry
November 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
January 17, 2024
CompletedJune 4, 2024
June 1, 2024
14 days
November 16, 2023
June 3, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Vizuel Analog Scala, (VAS)
VAS is an extremely simple, effective and repeatable measurement tool that requires minimal tools to measure both pain intensity and pain relief. It is a 10 cm long ruler drawn horizontally or vertically, starting with "No pain" and ending with "Unbearable pain". The patient is told to make a mark on this line that corresponds to the severity of his pain, intersecting this line. The distance from the lowest VAS level to the patient's mark is measured with a ruler to obtain a numerical index of the patient's pain intensity in cm or mm.
baseline, post-exercise (day 12)
Secondary Outcomes (1)
Fatigue Severity Scale, (FSS)
baseline, post-exercise (day 12)
Other Outcomes (4)
Functional independence measure, (FIM)
baseline, post-exercise (day 12)
State Anxiety Scale
baseline, post-exercise (day 12)
Functional Independence Measure for Children (WeeFIM)
baseline, post-exercise (day 12)
- +1 more other outcomes
Eligibility Criteria
Population/Sample of the Study: The population of the study consists of patients receiving Physiotherapy and Rehabilitation services in the hospital and rehabilitation center where the health services where the research will be carried out are provided. The sample of the research: Consists of 60 volunteer participants under the age of 18 and 177 participants over the age of 18 in the relevant units of three different health institutions, as stated, consisting of women and men. Only 89 female and male volunteer participants over the age of 18 will be included in the study in the physical therapy and rehabilitation unit of our hospital.
You may qualify if:
- Having a clinical problem that causes physiotherapy and rehabilitation treatment
- Being able to understand Turkish
You may not qualify if:
- Not wanting to participate in the study
- Having a chronic disease or disability that would prevent the application of the home program.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Necmettin Erbakan University
Konya, Meram, Turkey (Türkiye)
Related Publications (1)
Kim JY, Lee MK, Lee DH, Kang DW, Min JH, Lee JW, Chu SH, Cho MS, Kim NK, Jeon JY. Effects of a 12-week home-based exercise program on quality of life, psychological health, and the level of physical activity in colorectal cancer survivors: a randomized controlled trial. Support Care Cancer. 2019 Aug;27(8):2933-2940. doi: 10.1007/s00520-018-4588-0. Epub 2018 Dec 18.
PMID: 30564936BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Neslihan Altuntaş Yılmaz
Necmettin Erbakan University
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 12 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- doctor
Study Record Dates
First Submitted
November 16, 2023
First Posted
November 21, 2023
Study Start
November 17, 2023
Primary Completion
December 1, 2023
Study Completion
January 17, 2024
Last Updated
June 4, 2024
Record last verified: 2024-06